FDA.reportPublic FDA data

Benzethonium Chloride Solution

Manufacturer
The Dial Corporation, A Henkel Company | The Dial Corporation
Effective date
2014-12-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:57

Label at a glance#

ProductBenzethonium Chloride Solution
Active ingredientBENZETHONIUM CHLORIDE
Label structure17 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

KILLS MORE GERMS

Than Ordinary Liquid Hand Soap

Others*

After washing with other ordinary hand soap.

Dial Complete*

After washing with Dial Complete Foaming Antibacterial Hand Wash

*Dramatization only: Number of organisms shown does not reflect actual number of bacteria.

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride 0.20%

OTC - PURPOSE SECTION

Antibacterial

OTC - PURPOSE SECTION

Uses - For handwashing to decrease bacteria on the skin

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product - Avoid contact with eyes. In case of eye contact, flush with water.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or redness develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INSTRUCTIONS FOR USE SECTION

Directions

  • pump into DRY hands
  • lather vigorously for at least 15 seconds
  • rinse and dry thoroughly

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Glycerin, Lauramine Oxide, Fragrance, Punica Granatam Fruit Juice, Rubus Idaeus (Raspberry) Juice, Vaccinium Macrocarpon (Cranberry) Fruit Juice, Tocopheryl Acetate (Antioxidant), Camellia Oleifera (Green Tea) Leaf Extract (Antioxidant), Sunflowerseedamidopropyl Ethyldimonium Ethosulfate and PEG-9, Cocamidopropyl Betaine, Hydroxypropyl Methylcellulose, DMDM Hydantoin, Chlorhexidine Digluconate, Citric Acid, Zinc Sulfate, Tetrasodium EDTA, Red 33, Orange 4

SPL UNCLASSIFIED SECTION

* Encountered in household settings

** Antibacterial Liquid Hand Wash

REFILL ONLY WITH DIAL COMPLETE ® TOTAL CLEAN FORMULA

SPL UNCLASSIFIED SECTION

© 2014 & Distributed by THE DIAL CORPORATION
a Henkel COMPANY SCOTTSDALE, AZ 85255

Made in USA

The distinctive design and elements of this package are proprietary and
owned by The Dial Corporation, A Henkel Company

Patent Pending

DOSAGE & ADMINISTRATION SECTION

Topical Liquid

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kills 99.99% of Germs*

New Active!
TOTAL CLEAN FORMULA

Refill ONLY with Dial Complete® Total Clean Formula

Dial Complete® Foaming antibacterial Hand Wash

Gentle on skin

Power Berries

7.5 FL OZ (221mL)

DC Power Berries 7.5 ozDC Power Berries 7.5 oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1243889benzethonium chloride 0.2 % Medicated Liquid SoapPSN1
1243889benzethonium chloride 2 MG/ML Medicated Liquid SoapSCD1
1243889benzethonium chloride 0.2 % Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54340-251-012020-01-31C16284748780-19d75b9d0-de4f-f424-e053-dadaa90a57ceDial Complete Power Berries Foaming Antibacterial Hand Wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54340-251-01Benzethonium Chloride Solution221 mL in 1 BOTTLE, PUMPSOLUTION2211

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54340-251BENZETHONIUM CHLORIDE SOLUTION (DIAL COMPLETE POWER BERRIES FOAMING ANTIBACTERIAL HAND WASH) SOLUTION [THE DIAL CORPORATION, A HENKEL COMPANY]1Legacy NDC, 1 package rows20150313_0a70a80e-7b9f-6928-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZETHONIUM CHLORIDEACTIVE INGREDIENTPH41D057441
BENZETHONIUMACTIVE MOIETY1VU15B70BP1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54340-25154340-251-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZETHONIUM CHLORIDEPH41D05744ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0a70a80e-7ba0-6928-e054-00144ff8d46c0a70a80e-7b9f-6928-e054-00144ff8d46c2014-12-17WarningsExact identifier
spl id: 0a70a80e-7ba0-6928-e054-00144ff8d46c
spl set id: 0a70a80e-7b9f-6928-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.